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Kenorex

FDA UDI

Class II (US FDA UDI)

by Kentron Health Care, Inc.

Identity

Trade Name
KENOREX FDA UDI
Generic Name
Basic endotracheal tube, single-use FDA UDI
Device Name
ENDOTRACHEAL TUBE CUFFED 6.5 MM WITH SUCTION PORT MURPHY EYE FDA UDI
Model / Reference
919965 FDA UDI
Description
ENDOTRACHEAL TUBE CUFFED 6.5 MM WITH SUCTION PORT MURPHY EYE FDA UDI

Identifiers

Catalog Number
919965 FDA UDI
Primary DI / UDI-DI
00851785007599 FDA UDI
510(k) Number
K110269 FDA UDI
FDA Product Code
BTR FDA UDI
GMDN Term
Basic endotracheal tube, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5730 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Basic endotracheal tube, single-use

Kenorex by Kentron Health Care, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic endotracheal tube, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d6f7d97c-7e0d-43f6-99bc-95962dfc7d56 36 fields · synced May 30, 2026